Evidence map›Paper›PMID 23427141›Full record

ReviewAmerican journal of physiology. Renal physiology2013

Meprin A metalloproteinase and its role in acute kidney injury.

Gur P Kaushal, Randy S Haun, Christian Herzog, Sudhir V Shah

Abstract readReview
In one paragraph

Review in American journal of physiology. Renal physiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
4.2field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

34 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
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  6. Tissue Inhibitors of Metalloproteinase 1 (TIMP-1) and 3 (TIMP-3) as New Markers of Acute Kidney Injury After Massive Burns.Medical science monitor : international medical journal of experimental and clinical research · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Gur P KaushalCentral Arkansas Veterans Healthcare System, 4300 West 7th St., 111D/LR, Little Rock, AR 72205, USA. Kaushalgurp@uams.edu
Randy S Haun
Christian Herzog
Sudhir V Shah
University of Arkansas for Medical Sciences · USCentral Arkansas Veterans Healthcare System · US

Funding

Meprin A Metalloproteinase in Acute Kidney InjuryR01DK081690 · NIDDK · UNIV OF ARKANSAS FOR MED SCIS · PI KAUSHAL, GUR PRASAD · 2010 to 2013
$866k
Role of serine protease KLK7 in pancreatic cancerI01BX000828 · VA · CENTRAL ARKANSAS VETERANS HLTHCARE SYS · PI HAUN, RANDY S. · 2011 to 2014
–
BLRD VA I01 BX000828NIDDK NIH HHS DK-081690NIDDK NIH HHS R01 DK081690
6 · The paper itself

Abstract

Meprin A, composed of α- and β-subunits, is a membrane-associated neutral metalloendoprotease that belongs to the astacin family of zinc endopeptidases. It was first discovered as an azocasein and benzoyl-l-tyrosyl-p-aminobenzoic acid hydrolase in the brush-border membranes of proximal tubules and intestines. Meprin isoforms are now found to be widely distributed in various organs (kidney, intestines, leukocytes, skin, bladder, and a variety of cancer cells) and are capable of hydrolyzing and processing a large number of substrates, including extracellular matrix proteins, cytokines, adherens junction proteins, hormones, bioactive peptides, and cell surface proteins. The ability of meprin A to cleave various substrates sheds new light on the functional properties of this enzyme, including matrix remodeling, inflammation, and cell-cell and cell-matrix processes. Following ischemia-reperfusion (IR)- and cisplatin-induced acute kidney injury (AKI), meprin A is redistributed toward the basolateral plasma membrane, and the cleaved form of meprin A is excreted in the urine. These studies suggest that altered localization and shedding of meprin A in places other than the apical membranes may be deleterious in vivo in acute tubular injury. These studies also provide new insight into the importance of a sheddase involved in the release of membrane-associated meprin A under pathological conditions. Meprin A is injurious to the kidney during AKI, as meprin A-knockout mice and meprin inhibition provide protective roles and improve renal function. Meprin A, therefore, plays an important role in AKI and potentially is a unique target for therapeutic intervention during AKI.

Indexed as

Acute Kidney InjuryAnimalsCell MembraneDisease Models, AnimalEpithelial CellsHumansLeukocytesMetalloendopeptidasesMiceMice, KnockoutRatsmeprin AMetalloendopeptidasesacute kidney injurymeprinmetalloproteinaserenal proximal tubule

Identifiers

PMID23427141
PMCPMC3651633
OpenAlexW2048598064

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.